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Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study

Maternal pre-conception obesity is a strong risk factor for childhood overweight. However, prenatal mechanisms and their effects in susceptible gestational periods that contribute to this risk are not well understood. We aimed to assess the impact of late-pregnancy dysglycemia in obese pregnancies w...

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Published in:PLoS medicine 2018-10, Vol.15 (10), p.e1002681-e1002681
Main Authors: Gomes, Delphina, von Kries, Rüdiger, Delius, Maria, Mansmann, Ulrich, Nast, Martha, Stubert, Martina, Langhammer, Lena, Haas, Nikolaus A, Netz, Heinrich, Obermeier, Viola, Kuhle, Stefan, Holdt, Lesca M, Teupser, Daniel, Hasbargen, Uwe, Roscher, Adelbert A, Ensenauer, Regina
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creator Gomes, Delphina
von Kries, Rüdiger
Delius, Maria
Mansmann, Ulrich
Nast, Martha
Stubert, Martina
Langhammer, Lena
Haas, Nikolaus A
Netz, Heinrich
Obermeier, Viola
Kuhle, Stefan
Holdt, Lesca M
Teupser, Daniel
Hasbargen, Uwe
Roscher, Adelbert A
Ensenauer, Regina
description Maternal pre-conception obesity is a strong risk factor for childhood overweight. However, prenatal mechanisms and their effects in susceptible gestational periods that contribute to this risk are not well understood. We aimed to assess the impact of late-pregnancy dysglycemia in obese pregnancies with negative testing for gestational diabetes mellitus (GDM) on long-term mother-child outcomes. The prospective cohort study Programming of Enhanced Adiposity Risk in Childhood-Early Screening (PEACHES) (n = 1,671) enrolled obese and normal weight mothers from August 2010 to December 2015 with trimester-specific data on glucose metabolism including GDM status at the end of the second trimester and maternal glycated hemoglobin (HbA1c) at delivery as a marker for late-pregnancy dysglycemia (HbA1c ≥ 5.7% [39 mmol/mol]). We assessed offspring short- and long-term outcomes up to 4 years, and maternal glucose metabolism 3.5 years postpartum. Multivariable linear and log-binomial regression with effects presented as mean increments (Δ) or relative risks (RRs) with 95% confidence intervals (CIs) were used to examine the association between late-pregnancy dysglycemia and outcomes. Linear mixed-effects models were used to study the longitudinal development of offspring body mass index (BMI) z-scores. The contribution of late-pregnancy dysglycemia to the association between maternal pre-conception obesity and offspring BMI was estimated using mediation analysis. In all, 898 mother-child pairs were included in this unplanned interim analysis. Among obese mothers with negative testing for GDM (n = 448), those with late-pregnancy dysglycemia (n = 135, 30.1%) had higher proportions of excessive total gestational weight gain (GWG), excessive third-trimester GWG, and offspring with large-for-gestational-age birth weight than those without. Besides higher birth weight (Δ 192 g, 95% CI 100-284) and cord-blood C-peptide concentration (Δ 0.10 ng/ml, 95% CI 0.02-0.17), offspring of these women had greater weight gain during early childhood (Δ BMI z-score per year 0.18, 95% CI 0.06-0.30, n = 262) and higher BMI z-score at 4 years (Δ 0.58, 95% CI 0.18-0.99, n = 43) than offspring of the obese, GDM-negative mothers with normal HbA1c values at delivery. Late-pregnancy dysglycemia in GDM-negative mothers accounted for about one-quarter of the association of maternal obesity with offspring BMI at age 4 years (n = 151). In contrast, childhood BMI z-scores were not affected by a diagnosis o
doi_str_mv 10.1371/journal.pmed.1002681
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However, prenatal mechanisms and their effects in susceptible gestational periods that contribute to this risk are not well understood. We aimed to assess the impact of late-pregnancy dysglycemia in obese pregnancies with negative testing for gestational diabetes mellitus (GDM) on long-term mother-child outcomes. The prospective cohort study Programming of Enhanced Adiposity Risk in Childhood-Early Screening (PEACHES) (n = 1,671) enrolled obese and normal weight mothers from August 2010 to December 2015 with trimester-specific data on glucose metabolism including GDM status at the end of the second trimester and maternal glycated hemoglobin (HbA1c) at delivery as a marker for late-pregnancy dysglycemia (HbA1c ≥ 5.7% [39 mmol/mol]). We assessed offspring short- and long-term outcomes up to 4 years, and maternal glucose metabolism 3.5 years postpartum. Multivariable linear and log-binomial regression with effects presented as mean increments (Δ) or relative risks (RRs) with 95% confidence intervals (CIs) were used to examine the association between late-pregnancy dysglycemia and outcomes. Linear mixed-effects models were used to study the longitudinal development of offspring body mass index (BMI) z-scores. The contribution of late-pregnancy dysglycemia to the association between maternal pre-conception obesity and offspring BMI was estimated using mediation analysis. In all, 898 mother-child pairs were included in this unplanned interim analysis. Among obese mothers with negative testing for GDM (n = 448), those with late-pregnancy dysglycemia (n = 135, 30.1%) had higher proportions of excessive total gestational weight gain (GWG), excessive third-trimester GWG, and offspring with large-for-gestational-age birth weight than those without. Besides higher birth weight (Δ 192 g, 95% CI 100-284) and cord-blood C-peptide concentration (Δ 0.10 ng/ml, 95% CI 0.02-0.17), offspring of these women had greater weight gain during early childhood (Δ BMI z-score per year 0.18, 95% CI 0.06-0.30, n = 262) and higher BMI z-score at 4 years (Δ 0.58, 95% CI 0.18-0.99, n = 43) than offspring of the obese, GDM-negative mothers with normal HbA1c values at delivery. Late-pregnancy dysglycemia in GDM-negative mothers accounted for about one-quarter of the association of maternal obesity with offspring BMI at age 4 years (n = 151). In contrast, childhood BMI z-scores were not affected by a diagnosis of GDM in obese pregnancies (GDM-positive: 0.58, 95% CI 0.36-0.79, versus GDM-negative: 0.62, 95% CI 0.44-0.79). One mechanism triggering late-pregnancy dysglycemia in obese, GDM-negative mothers was related to excessive third-trimester weight gain (RR 1.72, 95% CI 1.12-2.65). Furthermore, in the maternal population, we found a 4-fold (RR 4.01, 95% CI 1.97-8.17) increased risk of future prediabetes or diabetes if obese, GDM-negative women had a high versus normal HbA1c at delivery (absolute risk: 43.2% versus 10.5%). There is a potential for misclassification bias as the predominantly used GDM test procedure changed over the enrollment period. Further studies are required to validate the findings and elucidate the possible third-trimester factors contributing to future mother-child health status. Findings from this interim analysis suggest that offspring of obese mothers treated because of a diagnosis of GDM appeared to have a better BMI outcome in childhood than those of obese mothers who-following negative GDM testing-remained untreated in the last trimester and developed dysglycemia. Late-pregnancy dysglycemia related to uncontrolled weight gain may contribute to the development of child overweight and maternal diabetes. Our data suggest that negative GDM testing in obese pregnancies is not an "all-clear signal" and should not lead to reduced attention and risk awareness of physicians and obese women. Effective strategies are needed to maintain third-trimester glycemic and weight gain control among otherwise healthy obese pregnant women.</description><identifier>ISSN: 1549-1676</identifier><identifier>ISSN: 1549-1277</identifier><identifier>EISSN: 1549-1676</identifier><identifier>DOI: 10.1371/journal.pmed.1002681</identifier><identifier>PMID: 30372451</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adipose tissue ; Biology and Life Sciences ; Birth weight ; Blood levels ; Body mass ; Body mass index ; Body weight ; Body weight gain ; Cardiology ; Childhood ; Children ; Children &amp; youth ; Cohort analysis ; Diabetes ; Diabetes mellitus ; Diagnosis ; Epidemiology ; Glucose ; Glucose metabolism ; Gynecology ; Health risk assessment ; Health risks ; Hemoglobin ; Hospitals ; Hyperglycemia ; Intensive care ; Laboratories ; Medical personnel ; Medicine ; Medicine and Health Sciences ; Metabolism ; Obesity ; Obstetrics ; Offspring ; Overweight ; Peaches ; Pediatrics ; Postpartum ; Pregnancy ; Risk factors ; Visualization ; Womens health</subject><ispartof>PLoS medicine, 2018-10, Vol.15 (10), p.e1002681-e1002681</ispartof><rights>2018 Gomes et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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However, prenatal mechanisms and their effects in susceptible gestational periods that contribute to this risk are not well understood. We aimed to assess the impact of late-pregnancy dysglycemia in obese pregnancies with negative testing for gestational diabetes mellitus (GDM) on long-term mother-child outcomes. The prospective cohort study Programming of Enhanced Adiposity Risk in Childhood-Early Screening (PEACHES) (n = 1,671) enrolled obese and normal weight mothers from August 2010 to December 2015 with trimester-specific data on glucose metabolism including GDM status at the end of the second trimester and maternal glycated hemoglobin (HbA1c) at delivery as a marker for late-pregnancy dysglycemia (HbA1c ≥ 5.7% [39 mmol/mol]). We assessed offspring short- and long-term outcomes up to 4 years, and maternal glucose metabolism 3.5 years postpartum. Multivariable linear and log-binomial regression with effects presented as mean increments (Δ) or relative risks (RRs) with 95% confidence intervals (CIs) were used to examine the association between late-pregnancy dysglycemia and outcomes. Linear mixed-effects models were used to study the longitudinal development of offspring body mass index (BMI) z-scores. The contribution of late-pregnancy dysglycemia to the association between maternal pre-conception obesity and offspring BMI was estimated using mediation analysis. In all, 898 mother-child pairs were included in this unplanned interim analysis. Among obese mothers with negative testing for GDM (n = 448), those with late-pregnancy dysglycemia (n = 135, 30.1%) had higher proportions of excessive total gestational weight gain (GWG), excessive third-trimester GWG, and offspring with large-for-gestational-age birth weight than those without. Besides higher birth weight (Δ 192 g, 95% CI 100-284) and cord-blood C-peptide concentration (Δ 0.10 ng/ml, 95% CI 0.02-0.17), offspring of these women had greater weight gain during early childhood (Δ BMI z-score per year 0.18, 95% CI 0.06-0.30, n = 262) and higher BMI z-score at 4 years (Δ 0.58, 95% CI 0.18-0.99, n = 43) than offspring of the obese, GDM-negative mothers with normal HbA1c values at delivery. Late-pregnancy dysglycemia in GDM-negative mothers accounted for about one-quarter of the association of maternal obesity with offspring BMI at age 4 years (n = 151). In contrast, childhood BMI z-scores were not affected by a diagnosis of GDM in obese pregnancies (GDM-positive: 0.58, 95% CI 0.36-0.79, versus GDM-negative: 0.62, 95% CI 0.44-0.79). One mechanism triggering late-pregnancy dysglycemia in obese, GDM-negative mothers was related to excessive third-trimester weight gain (RR 1.72, 95% CI 1.12-2.65). Furthermore, in the maternal population, we found a 4-fold (RR 4.01, 95% CI 1.97-8.17) increased risk of future prediabetes or diabetes if obese, GDM-negative women had a high versus normal HbA1c at delivery (absolute risk: 43.2% versus 10.5%). There is a potential for misclassification bias as the predominantly used GDM test procedure changed over the enrollment period. Further studies are required to validate the findings and elucidate the possible third-trimester factors contributing to future mother-child health status. Findings from this interim analysis suggest that offspring of obese mothers treated because of a diagnosis of GDM appeared to have a better BMI outcome in childhood than those of obese mothers who-following negative GDM testing-remained untreated in the last trimester and developed dysglycemia. Late-pregnancy dysglycemia related to uncontrolled weight gain may contribute to the development of child overweight and maternal diabetes. Our data suggest that negative GDM testing in obese pregnancies is not an "all-clear signal" and should not lead to reduced attention and risk awareness of physicians and obese women. Effective strategies are needed to maintain third-trimester glycemic and weight gain control among otherwise healthy obese pregnant women.</description><subject>Adipose tissue</subject><subject>Biology and Life Sciences</subject><subject>Birth weight</subject><subject>Blood levels</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Body weight</subject><subject>Body weight gain</subject><subject>Cardiology</subject><subject>Childhood</subject><subject>Children</subject><subject>Children &amp; youth</subject><subject>Cohort analysis</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diagnosis</subject><subject>Epidemiology</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Gynecology</subject><subject>Health risk assessment</subject><subject>Health risks</subject><subject>Hemoglobin</subject><subject>Hospitals</subject><subject>Hyperglycemia</subject><subject>Intensive care</subject><subject>Laboratories</subject><subject>Medical personnel</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Metabolism</subject><subject>Obesity</subject><subject>Obstetrics</subject><subject>Offspring</subject><subject>Overweight</subject><subject>Peaches</subject><subject>Pediatrics</subject><subject>Postpartum</subject><subject>Pregnancy</subject><subject>Risk factors</subject><subject>Visualization</subject><subject>Womens health</subject><issn>1549-1676</issn><issn>1549-1277</issn><issn>1549-1676</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUk1v1DAQjRCIlsI_QGCJC5csthM7CYdKVcVHpUpc4GxN7EniJRsvtrMof5Ffhbe7W7WIk8cz772Z0bwse83oihUV-7B2s59gXG03aFaMUi5r9iQ7Z6JsciYr-fRBfJa9CGGdMA1t6PPsrKBFxUvBzrM_txAx33rsJ5j0QswS-nHRuLFA7ERciwHJqWwxEOgiejJhD9HukEQM0U496ZwnfYpT1qWpiLHQYtzjJ0O8DT-J60g3x9kj0YMdzeCcIW6H_jfafogfydWUGiZtu0kcGJdgA-m8Sz8yuqm3cTZ2r7xxcUCf34kQ7QbnIwmpuLzMnnUwBnx1fC-yH58_fb_-mt9--3JzfXWba8FlzAGqGrGtoWoEikqzRla8Nth1uuYGywKN0Q2IFmoQpaCiZpI30lSiACErU1xkbw-629EFdTxDUJwLzgvZSJ4QNweEcbBW27QS-EU5sOou4XyvwEerR1SoW20ASqq7uiybspValm2nOW2MlrDXujx2m9t0aY1T9DA-En1cmeygerdTklMhZZEE3h8FvPs1pxOpjQ0axxEmdHOam_GKU1bQOkHf_QP9_3blAaW9C8Fjdz8Mo2pvzRNL7a2pjtZMtDcPF7knnbxY_AUC_OmA</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Gomes, Delphina</creator><creator>von Kries, Rüdiger</creator><creator>Delius, Maria</creator><creator>Mansmann, Ulrich</creator><creator>Nast, Martha</creator><creator>Stubert, Martina</creator><creator>Langhammer, Lena</creator><creator>Haas, Nikolaus A</creator><creator>Netz, Heinrich</creator><creator>Obermeier, Viola</creator><creator>Kuhle, Stefan</creator><creator>Holdt, Lesca M</creator><creator>Teupser, Daniel</creator><creator>Hasbargen, Uwe</creator><creator>Roscher, Adelbert A</creator><creator>Ensenauer, Regina</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>CZK</scope><orcidid>https://orcid.org/0000-0001-9417-3727</orcidid><orcidid>https://orcid.org/0000-0002-0724-5241</orcidid><orcidid>https://orcid.org/0000-0002-2420-6850</orcidid></search><sort><creationdate>20181001</creationdate><title>Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study</title><author>Gomes, Delphina ; von Kries, Rüdiger ; Delius, Maria ; Mansmann, Ulrich ; Nast, Martha ; Stubert, Martina ; Langhammer, Lena ; Haas, Nikolaus A ; Netz, Heinrich ; Obermeier, Viola ; Kuhle, Stefan ; Holdt, Lesca M ; Teupser, Daniel ; Hasbargen, Uwe ; Roscher, Adelbert A ; Ensenauer, Regina</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-aa78eeb8a795e57c196728deffc82de43eddc9a5ba8a54505816296d753a567d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adipose tissue</topic><topic>Biology and Life Sciences</topic><topic>Birth weight</topic><topic>Blood levels</topic><topic>Body mass</topic><topic>Body mass index</topic><topic>Body weight</topic><topic>Body weight gain</topic><topic>Cardiology</topic><topic>Childhood</topic><topic>Children</topic><topic>Children &amp; youth</topic><topic>Cohort analysis</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diagnosis</topic><topic>Epidemiology</topic><topic>Glucose</topic><topic>Glucose metabolism</topic><topic>Gynecology</topic><topic>Health risk assessment</topic><topic>Health risks</topic><topic>Hemoglobin</topic><topic>Hospitals</topic><topic>Hyperglycemia</topic><topic>Intensive care</topic><topic>Laboratories</topic><topic>Medical personnel</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Metabolism</topic><topic>Obesity</topic><topic>Obstetrics</topic><topic>Offspring</topic><topic>Overweight</topic><topic>Peaches</topic><topic>Pediatrics</topic><topic>Postpartum</topic><topic>Pregnancy</topic><topic>Risk factors</topic><topic>Visualization</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes, Delphina</creatorcontrib><creatorcontrib>von Kries, Rüdiger</creatorcontrib><creatorcontrib>Delius, Maria</creatorcontrib><creatorcontrib>Mansmann, Ulrich</creatorcontrib><creatorcontrib>Nast, Martha</creatorcontrib><creatorcontrib>Stubert, Martina</creatorcontrib><creatorcontrib>Langhammer, Lena</creatorcontrib><creatorcontrib>Haas, Nikolaus A</creatorcontrib><creatorcontrib>Netz, Heinrich</creatorcontrib><creatorcontrib>Obermeier, Viola</creatorcontrib><creatorcontrib>Kuhle, Stefan</creatorcontrib><creatorcontrib>Holdt, Lesca M</creatorcontrib><creatorcontrib>Teupser, Daniel</creatorcontrib><creatorcontrib>Hasbargen, Uwe</creatorcontrib><creatorcontrib>Roscher, Adelbert A</creatorcontrib><creatorcontrib>Ensenauer, Regina</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Academic</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><collection>PLoS Medicine</collection><jtitle>PLoS medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomes, Delphina</au><au>von Kries, Rüdiger</au><au>Delius, Maria</au><au>Mansmann, Ulrich</au><au>Nast, Martha</au><au>Stubert, Martina</au><au>Langhammer, Lena</au><au>Haas, Nikolaus A</au><au>Netz, Heinrich</au><au>Obermeier, Viola</au><au>Kuhle, Stefan</au><au>Holdt, Lesca M</au><au>Teupser, Daniel</au><au>Hasbargen, Uwe</au><au>Roscher, Adelbert A</au><au>Ensenauer, Regina</au><au>Myers, Jenny E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study</atitle><jtitle>PLoS medicine</jtitle><addtitle>PLoS Med</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>15</volume><issue>10</issue><spage>e1002681</spage><epage>e1002681</epage><pages>e1002681-e1002681</pages><issn>1549-1676</issn><issn>1549-1277</issn><eissn>1549-1676</eissn><abstract>Maternal pre-conception obesity is a strong risk factor for childhood overweight. However, prenatal mechanisms and their effects in susceptible gestational periods that contribute to this risk are not well understood. We aimed to assess the impact of late-pregnancy dysglycemia in obese pregnancies with negative testing for gestational diabetes mellitus (GDM) on long-term mother-child outcomes. The prospective cohort study Programming of Enhanced Adiposity Risk in Childhood-Early Screening (PEACHES) (n = 1,671) enrolled obese and normal weight mothers from August 2010 to December 2015 with trimester-specific data on glucose metabolism including GDM status at the end of the second trimester and maternal glycated hemoglobin (HbA1c) at delivery as a marker for late-pregnancy dysglycemia (HbA1c ≥ 5.7% [39 mmol/mol]). We assessed offspring short- and long-term outcomes up to 4 years, and maternal glucose metabolism 3.5 years postpartum. Multivariable linear and log-binomial regression with effects presented as mean increments (Δ) or relative risks (RRs) with 95% confidence intervals (CIs) were used to examine the association between late-pregnancy dysglycemia and outcomes. Linear mixed-effects models were used to study the longitudinal development of offspring body mass index (BMI) z-scores. The contribution of late-pregnancy dysglycemia to the association between maternal pre-conception obesity and offspring BMI was estimated using mediation analysis. In all, 898 mother-child pairs were included in this unplanned interim analysis. Among obese mothers with negative testing for GDM (n = 448), those with late-pregnancy dysglycemia (n = 135, 30.1%) had higher proportions of excessive total gestational weight gain (GWG), excessive third-trimester GWG, and offspring with large-for-gestational-age birth weight than those without. Besides higher birth weight (Δ 192 g, 95% CI 100-284) and cord-blood C-peptide concentration (Δ 0.10 ng/ml, 95% CI 0.02-0.17), offspring of these women had greater weight gain during early childhood (Δ BMI z-score per year 0.18, 95% CI 0.06-0.30, n = 262) and higher BMI z-score at 4 years (Δ 0.58, 95% CI 0.18-0.99, n = 43) than offspring of the obese, GDM-negative mothers with normal HbA1c values at delivery. Late-pregnancy dysglycemia in GDM-negative mothers accounted for about one-quarter of the association of maternal obesity with offspring BMI at age 4 years (n = 151). In contrast, childhood BMI z-scores were not affected by a diagnosis of GDM in obese pregnancies (GDM-positive: 0.58, 95% CI 0.36-0.79, versus GDM-negative: 0.62, 95% CI 0.44-0.79). One mechanism triggering late-pregnancy dysglycemia in obese, GDM-negative mothers was related to excessive third-trimester weight gain (RR 1.72, 95% CI 1.12-2.65). Furthermore, in the maternal population, we found a 4-fold (RR 4.01, 95% CI 1.97-8.17) increased risk of future prediabetes or diabetes if obese, GDM-negative women had a high versus normal HbA1c at delivery (absolute risk: 43.2% versus 10.5%). There is a potential for misclassification bias as the predominantly used GDM test procedure changed over the enrollment period. Further studies are required to validate the findings and elucidate the possible third-trimester factors contributing to future mother-child health status. Findings from this interim analysis suggest that offspring of obese mothers treated because of a diagnosis of GDM appeared to have a better BMI outcome in childhood than those of obese mothers who-following negative GDM testing-remained untreated in the last trimester and developed dysglycemia. Late-pregnancy dysglycemia related to uncontrolled weight gain may contribute to the development of child overweight and maternal diabetes. Our data suggest that negative GDM testing in obese pregnancies is not an "all-clear signal" and should not lead to reduced attention and risk awareness of physicians and obese women. Effective strategies are needed to maintain third-trimester glycemic and weight gain control among otherwise healthy obese pregnant women.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>30372451</pmid><doi>10.1371/journal.pmed.1002681</doi><orcidid>https://orcid.org/0000-0001-9417-3727</orcidid><orcidid>https://orcid.org/0000-0002-0724-5241</orcidid><orcidid>https://orcid.org/0000-0002-2420-6850</orcidid><oa>free_for_read</oa></addata></record>
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subjects Adipose tissue
Biology and Life Sciences
Birth weight
Blood levels
Body mass
Body mass index
Body weight
Body weight gain
Cardiology
Childhood
Children
Children & youth
Cohort analysis
Diabetes
Diabetes mellitus
Diagnosis
Epidemiology
Glucose
Glucose metabolism
Gynecology
Health risk assessment
Health risks
Hemoglobin
Hospitals
Hyperglycemia
Intensive care
Laboratories
Medical personnel
Medicine
Medicine and Health Sciences
Metabolism
Obesity
Obstetrics
Offspring
Overweight
Peaches
Pediatrics
Postpartum
Pregnancy
Risk factors
Visualization
Womens health
title Late-pregnancy dysglycemia in obese pregnancies after negative testing for gestational diabetes and risk of future childhood overweight: An interim analysis from a longitudinal mother-child cohort study
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